FDA UDI In Commercial Distribution 🇺🇸 United States

PENTAX Medical

DI: 04961333246632 · Model: ED32-i10 · HOYA CORPORATION
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
PENTAX Medical
Primary DI
04961333246632
Version / Model
ED32-i10
Company Name
HOYA CORPORATION
Labeler DUNS
691519705
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-02
Public Version
3
Public Version Date
2023-11-30
Public Version Status
Update
Public Device Record Key
2f008ece-3934-48b3-b9cb-7f60fce51d00

Device Description

PENTAX Medical Video Duodenoscope ED32-i10

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
Yes
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
["High-level Disinfectant", "Liquid Chemical"]

Product Codes

Code Name
FDT duodenoscope and accessories, flexible/rigid

GMDN Terms

Code Name
36112 Flexible video duodenoscope, reusable

Identifiers

Type ID
Direct Marking 04961333246168
Primary 04961333246632

Premarket Submissions

Submission Number Supplement Number
K202365 000